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Pathophysiology study sheet
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An alphabetized list. See if you know them all!
(completed sheet is available on the yahoogroup)
EXAM 3 PATHOPHYSIOLOGY LIST
Aceruloplasminemia
Alkaptonuria
Anderson’s Disease
Anemia
Anemia of Chronic Disease
Angina
Arteriosclerosis
Atherosclerosis
Beri-beri
Branched chain keto aciduria
Cancer and RAS
Cholera
Crigler-Najjar Syndrome
Cystinosis
Cystinuria
Diabetes
Dyslipidemia
End-stage kidney disorder (and RBC production)
Elevated NH3
Enzymopathies
Essential Fructose Uria
Farnesylation of RAS
Gaucher’s Disease
Gilbert’s syndrome
Glucose 6-Phosphate Dehydrogenase Deficiency
Hartnup’s Disease
Hemoglobin C disease
Hemoglobinopathies
Hemolysis
Hemorrhage
Hereditary elliptocytosis / pyropoikilocytosis
Hereditary Hemochromatosis
Hereditary Fructose Intolerance
Hereditary Spherocytosis
Hexokinase deficiency
Homocystinuria
Homocysteinemia
Hyperbilirubinemia
Hypoxia
21-Hydroxylase deficiency
Infection and Inflammation
Inherited Galactosemia
Iron deficiency anemia
Jaundice
Lead Poisoning
Lipoprotein (a) increase
Marasmus
McArdle’s disease
Membranopathies
Metabolic Acidosis
Metabolic syndrome
Methemoglobin Anemia
Myocardial Infaction (MI)
Niemann-Pick Disease (Type A)
Obesity
Osteomalacia
Pellegra
Pernicious Anemia
Phenylketonuria
Polycythemia
Porphyrias
Pregnancy (and iron)
Protein-Energy Malnutrition (P.E.M.)
Pseudothrombocytopenia
Pyruvate kinase deficiency
Rickets
Sickle cell anemia
Small Dense LDL
Scurvy
Southeast Asian Ovalocytosis (SAO)
Splenectomy (consequences of…)
Steatorrhea
Stenosis
Stroke
Tay-Sach’s disease
Trauma (and clot risk)
Thalasemia
Thrombocytopenia
Thrombosis
Urea cycle disorders
Van Gierke’s Disease
Vitamin A deficiency
Wernicke-Korsakoft
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(completed sheet is available on the yahoogroup)
EXAM 3 PATHOPHYSIOLOGY LIST
Aceruloplasminemia
Alkaptonuria
Anderson’s Disease
Anemia
Anemia of Chronic Disease
Angina
Arteriosclerosis
Atherosclerosis
Beri-beri
Branched chain keto aciduria
Cancer and RAS
Cholera
Crigler-Najjar Syndrome
Cystinosis
Cystinuria
Diabetes
Dyslipidemia
End-stage kidney disorder (and RBC production)
Elevated NH3
Enzymopathies
Essential Fructose Uria
Farnesylation of RAS
Gaucher’s Disease
Gilbert’s syndrome
Glucose 6-Phosphate Dehydrogenase Deficiency
Hartnup’s Disease
Hemoglobin C disease
Hemoglobinopathies
Hemolysis
Hemorrhage
Hereditary elliptocytosis / pyropoikilocytosis
Hereditary Hemochromatosis
Hereditary Fructose Intolerance
Hereditary Spherocytosis
Hexokinase deficiency
Homocystinuria
Homocysteinemia
Hyperbilirubinemia
Hypoxia
21-Hydroxylase deficiency
Infection and Inflammation
Inherited Galactosemia
Iron deficiency anemia
Jaundice
Lead Poisoning
Lipoprotein (a) increase
Marasmus
McArdle’s disease
Membranopathies
Metabolic Acidosis
Metabolic syndrome
Methemoglobin Anemia
Myocardial Infaction (MI)
Niemann-Pick Disease (Type A)
Obesity
Osteomalacia
Pellegra
Pernicious Anemia
Phenylketonuria
Polycythemia
Porphyrias
Pregnancy (and iron)
Protein-Energy Malnutrition (P.E.M.)
Pseudothrombocytopenia
Pyruvate kinase deficiency
Rickets
Sickle cell anemia
Small Dense LDL
Scurvy
Southeast Asian Ovalocytosis (SAO)
Splenectomy (consequences of…)
Steatorrhea
Stenosis
Stroke
Tay-Sach’s disease
Trauma (and clot risk)
Thalasemia
Thrombocytopenia
Thrombosis
Urea cycle disorders
Van Gierke’s Disease
Vitamin A deficiency
Wernicke-Korsakoft